共查询到20条相似文献,搜索用时 31 毫秒
1.
A magnetic‐sulfonic graphene nanocomposite (G‐SO3H/Fe3O4) was synthesized and characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X‐ray diffraction. It was used for removal of three cationic dyes: safranine T (ST), neutral red (NR), victoria blue (VB), and three anionic dyes: methyl orange, brilliant yellow, and alizarin red, from environmental water. The experimental conditions were optimized, including pH, amount of adsorbent, adsorption kinetics, adsorption isotherms, ionic strength, etc. The results show that G‐SO3H/Fe3O4 can adsorb cationic dyes more efficiently and selectively than anionic dyes at pH 6.0. In the first 10 min of adsorption time, more than 93% of the cationic dyes were removed by the sorbent. Adsorption kinetics follow the pseudo‐second‐order kinetic model well. The adsorption isotherm coincided with Langmuir and Freundlich adsorption models. The maximum adsorption capacities of G‐SO3H/Fe3O4 for ST, NR, and VB dyes were 199.3, 216.8, and 200.6 mg g?1. The adsorbed cationic dyes were eluted by using different pH values of ethanol as the solvent. The established method was simple, sensitive, and rapid, and was suitable for the adsorption of cationic dyes in environmental water. 相似文献
2.
The present work focuses on the performance of Fenton, sono‐Fenton, and sono‐photo‐Fenton processes for the oxidation of phenol present in aqueous solution. The effects of H2O2 concentration, Fe2+ concentration, pH, and initial phenol concentration on the oxidation of phenol were studied. The optimum Fe2+ and H2O2 concentrations for the Fenton process were 45 and 800 mg/L, respectively. For the sono‐Fenton process, the optimum Fe2+ and H2O2 concentrations were 30 and 800 mg/L, respectively. The optimal conditions for the sono‐photo‐Fenton process were found to be 20 mg/L of Fe2+ and 700 mg/L of H2O2. The optimum pH was found to be 3 for the processes investigated in the present study. The analysis of results showed that the sono‐photo‐Fenton method reduced the Fe2+ concentration by 30–50% and the H2O2 concentration by 12.5%. It was found that the sono‐photo‐Fenton technique showed better performance than the Fenton and sono‐Fenton processes for the oxidation of phenol. A lumped kinetic model was used to predict the chemical oxygen demand reduction and the model was found to fit the data. 相似文献
3.
In this study, the oxidative decolorization of C.I. reactive yellow 145 (RY 145) from synthetic textile wastewater including RY 145 and polyvinyl alcohol by Fenton and sono‐Fenton processes which are the combination of Fenton process with ultrasound has been carried out. The effects of some operating parameters which are the initial pH of the solution, the initial concentration of Fe2+, H2O2, and the dye, temperature, and agitation speed on the color and chemical oxygen demand (COD) removals have been investigated. The optimum conditions have been found as [Fe2+] = 20 mg/L, [H2O2] = 20 mg/L, pH 3 for Fenton process and [Fe2+] = 20 mg/L, [H2O2] = 15 mg/L, pH 3 for sono‐Fenton process by indirectly sonication at 35 kHz ultrasonic frequency and 80 W ultrasonic power. The color and COD removal efficiencies have been obtained as 91 and 47% by Fenton process, and 95 and 51% by sono‐Fenton processes, respectively. Kinetic studies have been performed for the decolorization of RY 145 under optimum conditions at room temperature. It has been determined that the decolorization has occurred rapidly by sono‐Fenton process, compared to Fenton process. 相似文献
4.
Celalettin Özdemir Hayrunnisa Tezcan Serkan Sahinkaya Erkan Kalipci 《洁净——土壤、空气、水》2010,38(12):1152-1158
The removal of chemical oxygen demand (COD) and phenol from olive oil mill wastewaters (OOMW) was investigated experimentally by using conventional Fenton (CFP) and Fenton type processes (FTP) with zero valent iron (ZVI). Different operational parameters such as initial pH, Fe2+, Fe0, and H2O2 concentrations were examined. Kinetic studies in terms of COD and phenol removals for both CFP and FTP were performed. The original pH value (4.6) of OOMW for CFP was found as the optimum pH. The determined optimum conditions are [Fe2+] = 1500 mg L?1, [H2O2] = 1750 mg L?1, and pH = 4.6 for CFP; [Fe0] = 2000 mg L?1, [H2O2] = 2000 mg L?1, and pH = 3 for FTP. 82.4% COD and 62% phenol removals were performed under the optimum conditions by CFP, while 82% COD and 63.4% phenol were removed by FTP. According to the results of kinetic studies, it was observed that COD and phenol were removed by FTP more rapidly, compared to CFP. Consequently, it was determined that both CFP and FTP were effective processes for the pretreatment of OOMW. 相似文献
5.
A simple and rapid soft‐templating coupled with one‐pot solvent thermal method is developed to synthesize S‐doped magnetic mesoporous carbon (S‐doped MMC). In this method, phenolic resin is used as a carbon precursor and Pluronic copolymer P123 is used as a template and 2,5‐dimercapto‐1,3,4‐thiadiazole is used as sulfur source. Prepared S‐doped MMC processes a high specific surface area, the Fe3O4 particles are well embedded in the mesoporous carbon walls that exhibit a strong magnetic response, and the hydrated iron nitrate loading amount of 0.808 g is the best. Batch adsorption experiments are carried out at different pH, initial concentration, temperature, and contact time on the adsorption of methyl orange (MO) by S‐doped MMC. The kinetic data of the adsorption process are better fitted with pseudo‐second‐order model than the pseudo‐first‐order model. Langmuir model is more suitable for the equilibrium data than Freundlich model. The thermodynamic parameters including ΔG0, ΔH0, and ΔS0 indicate that the adsorption is a feasible, spontaneous, and endothermic process. Finally, it is found that the coexistence of PO43?, NO3?, SO42?, Cl?, and CO32? does not influence the adsorption process. These results illustrate S‐doped MMC can be an efficient adsorbent for the removal of MO from wastewater. 相似文献
6.
The aim of this research was to decompose isoproturon and adsorb its photoproducts by developing a carbon material from a juice industry waste. Carbon-TiO2 hybrid materials were obtained by impregnating carbonized guava seeds with TiO2 gels prepared from TiOSO4⋅xH2O and NH4OH using glycerol as a binder and thermally treating the materials at 500 °C. Raman studies confirmed the anatase phase of TiO2. SEM images showed isolated TiO2 agglomerates firmly attached to the carbon surface. The adsorption behavior of isoproturon on guava carbon was studied and yielded S-type adsorption isotherms. The photocatalytic activities of the prepared hybrid materials were monitored to study the kinetics and elimination process both of the herbicide and its photoproducts. The reaction was monitored by UV–Vis spectrophotometry, LC-DAD and LC-MS, enabling identification of some intermediate species. Among the photoproducts produced by carbon-TiO2 hybrid materials, amino-isopropylphenol was detected. 相似文献
7.
Maedeh Galehdar Habibollah Younesi Mojtaba Hadavifar Ali Akbar Zinatizadeh 《洁净——土壤、空气、水》2009,37(8):629-637
In the present study, the effects of initial COD (chemical oxygen demand), initial pH, Fe2+/H2O2 molar ratio and UV contact time on COD removal from medium density fiberboard (MDF) wastewater using photo‐assisted Fenton oxidation treatment were investigated. In order to optimize the removal efficiency, batch operations were carried out. The influence of the aforementioned parameters on COD removal efficiency was studied using response surface methodology (RSM). The optimal conditions for maximum COD removal efficiency from MDF wastewater under experimental conditions were obtained at initial COD of 4000 mg/L, Fe2+/H2O2 molar ratio of 0.11, initial solution pH of 6.5 and UV contact time of 70 min. The obtained results for maximum COD removal efficiency of 96% revealed that photo‐assisted Fenton oxidation is very effective for treating MDF wastewater. 相似文献
8.
Bilsen Tural 《洁净——土壤、空气、水》2010,38(4):321-327
A novel, simple method based on magnetic separation was developed for analytical purposes. In this method, N‐methyl‐D‐glucamine (NMDG) modified magnetic microparticles that were synthesized by using the sol‐gel method were used for the selective extraction and preconcentration of boron from aqueous solutions. This method combines the simplicity and selectivity of solvent extraction with the easy separation of magnetic microparticles from a solution with a magnet without any preliminary filtration step. The structure of the prepared γ‐Fe2O3‐SiO2‐NMDG (magnetic sorbent) composites were characterized by using X‐ray diffraction (XRD), Transmission Electron Microscopy (TEM), and Fourier Transform Infrared Spectroscopy (FTIR). The influence of different parameters on the sorbent capacity, such as the sorption/desorption of boron, magnetic sorbent dosage, pH, equilibrium time, type, and amount of stripping solution, were evaluated by using the magnetic sorbent. Any equilibrium pH greater than 6 can be used for sorption. Desorption from the sorbent was carried out by using 1.0 M HCl. The sorption and desorption efficiency of the γ‐Fe2O3‐SiO2‐NMDG was found as 92.5 ± 0.5% and 99.8 ± 6%, respectively. 相似文献
9.
In this study, a new material consisting of activated‐carbon‐containing magnetic oxide is prepared for assisted microwave (MW) irradiation treatment of coking wastewater. The optimum condition for degrading coking wastewater is 98.14% chemical oxygen demand (COD), under which 87.57% ammonia nitrogen (NH3–N) can be removed. The results are verified by GC–MS, showing that most organic pollutants can be adsorbed by modified activated carbon (MAC). The surface morphology and elemental composition of MAC before and after microwave irradiation and adsorption is determined by scanning electron microscopy. After microwave irradiation, many apertures of pores looked relatively large. It can be shown that MAC as a catalyst in the microwave‐assisted treatment process has many advantages, including rapid degradation of COD and NH3–N. In conclusion, microwave‐irradiation‐assisted MAC treatment of coking wastewater is a novel technology that is economical, efficient, and has broad prospects for development. 相似文献
10.
This study attempts to explore the possibility of treating dye solutions containing Disperse Yellow 119 and Disperse Red 167 by Fenton and Fenton under solar‐light oxidation processes. Experiments were conducted to examine the effects of various operating conditions on the performance of the treatment systems. The Fenton results showed that 98.6% spectral absorption coefficient (SAC) and 90.8% chemical oxygen demand (COD) removals were proved at pH 3, 50 mg/L Fe2+, and 75 mg/L H2O2, 15 min oxidation time for Disperse Yellow 119. After 40 min solar irradiation time during Fenton process the SAC removal was 99.1%. COD reduction of about 98.3% was observed at the same time. It was also obtained as 97.8% SAC and 97.7% COD removal with pH 3, 75 mg/L Fe2+, 100 mg/L H2O2, and 25 min oxidation time for Disperse Red 167 at this optimum conditions. For Disperse Red 167 during Fenton under solar light process, after 40 min of solar irradiation time the SAC and COD reduction were obtained 99.3 and 98.4%, respectively. 相似文献
11.
Robert A. Berner 《Earth and Planetary Science Letters》1973,18(1):77-86
Chemical data presented in this paper indicate a good correlation between P2O5 and Fe2O3 in some iron-rich volcanogenic sediments from the East Pacific Rise. In addition, adsorption experiments and chemical analyses of deuterically altered and unaltered samples of submarine basalts strongly suggest that this association is due to the reaction of phosphate in sea water with poorly crystallized hydrous ferric oxides. East Pacific Rise sediments adsorb far greater amounts of phosphate from sea water than either carbonate or non-carbonate sediments from other areas of the ocean. From geochemical flux calculations it is concluded that an appreciable proportion of dissolved phosphate delivered to the oceans by rivers is removed by ridge crest volcanogenic iron oxides either as absorbed surface coatings or as discrete, but highly disordered, ferric phosphate phases. This process should be taken into consideration when considering oceanic phosphate budgets, both in the present and past oceans. 相似文献
12.
Spinel Ferrite Mediated Photo‐Fenton Degradation of Phenolic Analogues: A Detailed Study Employing Two Distinct Inorganic Oxidants
下载免费PDF全文
![点击此处可从《洁净——土壤、空气、水》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The present work demonstrates the applicability of ferrites as photo‐Fenton catalysts for deterioration of different phenolic derivatives. To analyze optimal reaction conditions, experiments are performed with four magnetic spinel ferrites MFe2O4 (M = Co, Cu, Ni, and Zn) and two inorganic oxidants, i.e., hydrogen peroxide (HP) and potassium peroxymonosulfate (PMS). The reactions are performed using p‐nitrophenol as phenolic probe. CuFe2O4 and CoFe2O4 possessed excellent ability to activate HP and PMS, respectively, among all four synthesized catalysts. A noteworthy aspect of two oxidizing agents is that the concentration of PMS used during the reaction is four times less than HP. Further, the broad pH activity of PMS provides a significant advantage over HP. The optimal reaction conditions, when HP is the oxidant in the photo‐Fenton degradation, are 0.50 g L?1 MFe2O4, pH 2.5, and 8.8 mM HP. Although PMS is active in a wide pH range (2–10), adequate reaction conditions are 0.50 g L?1 MFe2O4, natural pH, and 2.2 mM PMS. The photo‐Fenton activity of ferrites is extended to the degradation of different nitro‐ and chloro‐analogs of phenol (2‐nitrophenol, 3‐nitrophenol, 4‐nitrophenol, 2,4‐dinitrophenol, 2,4,6‐trinitrophenol, 2‐chlorophenol, 3‐chlorophenol, 4‐chlorophenol, 2,4‐dichlorophenol) with only two ferrites (CuFe2O4 and CoFe2O4). A comparative study is performed with the two oxidants (HP and PMS) with positive results. Finally, stability and reusability of magnetic ferrites as catalysts are also studied to prove their use in phenolic solution treatment. 相似文献
13.
Silvia Román João Manuel Valente Nabais Juan Félix González Carmen María González‐García Angel Luis Ortiz 《洁净——土壤、空气、水》2012,40(7):698-705
The adsorption of fluoxetine onto activated carbons (ACs) prepared from almond tree pruning by steam and CO2 activation under different temperature conditions (650–950°C), was studied. In both series increasing the temperature caused an increase in the BET apparent surface area, yielding ACs with SBET up to 870 and 710 m2 g?1 after steam and CO2 activation, respectively. Also, a slight widening of the porosity was found in both cases. In order to modify the functionality of the ACs, two of them were impregnated with triethylenediamine (TEDA) prior to the adsorption process, which caused a decrease in the AC apparent surface mainly due to micropore blockage. The fluoxetine adsorption isotherms at 25°C showed maximum adsorption capacities between 110 and 224 mg g?1. The adsorption isotherms were analyzed using Langmuir and Freundlich models. Although the impregnation reduced the pore volume, it did not cause a decrease in the fluoxetine maximum adsorption capacity, but a modification in the adsorption mechanism was observed. 相似文献
14.
《Physics of the Earth and Planetary Interiors》1999,110(1-2):43-50
The transformation of acicular γ Fe2O3 particles to α Fe2O3 has been monitored using magnetic properties as a proxy for γ Fe2O3 concentration during the inversion process. The transformation is thermally activated, the height of the barrier opposing inversion being 3.7 eV at atmospheric pressure and 0.5 eV at a pressure of about 100 MPa. The barrier arises from the combination of a term representing the reduction in lattice energy in an inverted region, and the strain energy associated with the interface between the inverted and non-inverted phases. The sensitivity of the inversion process to pressure can be understood in terms of the dependence of these energy terms, and the energy barrier, on interatomic spacing. Extrapolation of these laboratory data to the conditions of the submarine crust at Site 504B of the Deep Sea Drilling Project is consistent with the inferred magnetic mineralogy of the recovered material. 相似文献
15.
A chemical-physical method for treatment of aniline containing waste water was developed. At the chemical stage aniline is polymerized by Fenton's reagent. Thus insoluble polyaniline precipitates. The best reaction conditions are: pH-value of 2–3, stepwise dosing of 60 mL H2O2 (30%) and 12 mL saturated FeSO4-solution per litre waste water. The molar ratio Fe(II): H2O2 amounts to 0.3:10. The concentration of aniline is reduced by this chemical treatment from about 20 g/L to 30–40 mg/L. By adsorption at activated charcoal the concentration of aniline can be reduced further to 0.2 mg/L. The resulting sludge can easily be dewatered in a chamber filter press. 相似文献
16.
D.E. Watson E.E. Larson J.M. Herndon M.W. Rowe 《Earth and Planetary Science Letters》1975,27(1):101-107
Samples of all eighteen of the known C2 chondrites have been analyzed thermomagnetically. For eleven of these, initial Fe3O4 content is low (generally <1%) and theJs-T curves are irreversible. The heating curves show variable greater (up to 10 times) than it is initially. This behavior is attributed to the production of magnetite from a thermally unstable phase — apparently FeS. Four of the remaining seven C2 chondrites contain Fe3O4 as the only significant magnetic phase: initial magnetite contents range from 4 to 13%. The remaining three C2 chondrites contain iron or nickel-iron in addition to Fe3O4. These seven C2 chondrites show little evidence of the breakdown of a thermally unstable phase. 相似文献
17.
A suite of synthetic titanomagnetites of composition Fe2.4?δAlδTi0.6O4 and Fe2.6?δAlδTi0.4O4 (δ = 0, 0.1 and 0.2 in both cases) have been prepared by a method of partial self-buffering and pulverized in a ball mill to particle size of about 200–500 Å. Magnetic hysteresis parameters-saturation and remanent magnetizations and coercive force were measured between room temperature and the Curie temperatures and other parameters-X-ray cell edge, initial susceptibility and coercive force of remanence were determined at room temperature. The intrinsic magnetic “hardness” increases with increasing content of Al3+ and Ti4+, both probably corresponding to an increase in the concentration of Fe2+ ions on the tetrahedral sites of the spinel structure. The room-temperature hysteresis properties were compared with those resulting from monodomain models for the work done to magnetically saturate an assemblage of grains and the approach to saturation, and the separate contributions from coexisting anisotropies of cubic and uniaxial symmetries (assumed present) inferred. The cubic anisotropy energy constants so derived are larger than those determined from multidomain single crystals. The derived cubic constants are also larger than the derived uniaxial anisotropy constants. The latter, however, dominate the behaviour (e.g., coercive force) because of the lower symmetry. The materials appear to be entirely in the stable monodomain state at room temperature. 相似文献
18.
N. Thinakaran P. Baskaralingam K. V. Thiruvengada Ravi P. Panneerselvam Subramanian Sivanesan 《洁净——土壤、空气、水》2008,36(9):798-804
Activated carbons prepared from sunflower seed hull have been used as adsorbents for the removal of acid blue 15 (AB‐15) from aqueous solution. Batch adsorption techniques were performed to evaluate the influences of various experimental parameters, e. g., temperature, adsorbent dosage, pH, initial dye concentration and contact time on the adsorption process. The optimum conditions for AB‐15 removal were found to be pH = 3, adsorbent dosage = 3 g/L and equilibrium time = 4 h at 30°C. The adsorption of AB‐15 onto the adsorbent was found to increase with increasing dosage. It was found from experimental results that the Langmuir isotherm fits the data better than the Freundlich and Temkin isotherms. The maximum adsorption capacity, Qm (at 30°C) was calculated for SF1, SF2, and SF3 as 75, 125 and 110 mg g–1 of adsorbent, respectively. It was found that the adsorption follows pseudo‐second order kinetics. The thermodynamic parameters such as ΔG°, ΔH°, and ΔS° were also evaluated. The activated carbons prepared were characterized by FT‐IR, SEM and BET analysis. 相似文献
19.
In this paper, a novel composite material the silica grafted by poly(N‐vinyl imidazole) (PVI), i.e., PVI/SiO2, was prepared using 3‐methacryloxypropyl trimethoxysilane (MPS) as intermedia through the “grafting from” method. The adsorption behavior of metal ions by PVI/SiO2 was researched by both static and dynamic methods. Experimental results showed that PVI/SiO2 possessed very strong adsorption ability for metal ions. For different metal ions, PVI/SiO2 exhibited different adsorption abilities with the following order of adsorption capacity: Cu2+ > Cd2+ > Zn2+. The adsorption material PVI/SiO2 was especially good at adsorbing Cu(II) ion and the saturated adsorption capacity could reach up to 49.2 mg/g. The empirical Freundlich isotherm was found to describe well the equilibrium adsorption data. Higher temperatures facilitated the adsorption process and thus increased the adsorption capacity. The pH and grafting amount of PVI had great influence on the adsorption amount. In addition, PVI/SiO2 particles had excellent eluting and regenerating property using diluted hydrochloric acid solution as eluent. The adsorption ability trended to steady during 10 cycles. 相似文献
20.
Due to the unique chemical properties and therefore wide range of applications, significant amounts of reactive dyes often end up in waste waters and this issue raises the need for more efficient treatment technologies. This work investigates the ability of magnetite nanoparticles functionalized with imidazolium based ionic liquid (IL) as an efficient sorbent for the removal of the Reactive black 5 from wastewater. Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscopy, thermo‐gravimetric analysis, and zeta potential measurement were used to characterize the synthesized nanosorbent. The results showed that under optimal conditions, the dye removal efficiency of the grafted IL is 98.5% after a single run. Regeneration of the used sorbent could be possible and the modified magnetic nanoparticles exhibited good reusability. The isothermal data of RB5 sorption conformed well to the Langmuir model and the maximum sorption capacity of IL@Fe3O4 for RB5 was 161.29 mg g?1. Thermodynamic study indicated that the adsorption is endothermic and spontaneous. The use of such a system can provide fast and efficient removal of the reactive dyes from wastewater by using an external magnetic field. 相似文献